Literature DB >> 1945865

Poly (T/A) polymorphism at the human retinal degeneration slow (RDS) locus.

R Kumar-Singh1, S A Jordan, G J Farrar, P Humphries.   

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Year:  1991        PMID: 1945865      PMCID: PMC329011          DOI: 10.1093/nar/19.20.5800

Source DB:  PubMed          Journal:  Nucleic Acids Res        ISSN: 0305-1048            Impact factor:   16.971


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  2 in total

1.  The human retinal degeneration slow (RDS) gene: chromosome assignment and structure of the mRNA.

Authors:  G H Travis; L Christerson; P E Danielson; I Klisak; R S Sparkes; L B Hahn; T P Dryja; J G Sutcliffe
Journal:  Genomics       Date:  1991-07       Impact factor: 5.736

2.  Autosomal dominant retinitis pigmentosa: a new multi-allelic marker (D3S621) genetically linked to the disease locus (RP4).

Authors:  R Kumar-Singh; D G Bradley; G J Farrar; M Lawler; S A Jordan; P Humphries
Journal:  Hum Genet       Date:  1991-03       Impact factor: 4.132

  2 in total
  5 in total

1.  A new autosomal recessive retinitis pigmentosa locus maps on chromosome 2q31-q33.

Authors:  M Bayés; B Goldaracena; A Martínez-Mir; M I Iragui-Madoz; T Solans; P Chivelet; E Bussaglia; M A Ramos-Arroyo; M Baiget; L Vilageliu; S Balcells; R Gonzàlez-Duarte; D Grinberg
Journal:  J Med Genet       Date:  1998-02       Impact factor: 6.318

2.  Autosomal dominant retinitis pigmentosa (adRP; RP6): cosegregation of RP6 and the peripherin-RDS locus in a late-onset family of Irish origin.

Authors:  S A Jordan; G J Farrar; R Kumar-Singh; P Kenna; M M Humphries; V Allamand; E M Sharp; P Humphries
Journal:  Am J Hum Genet       Date:  1992-03       Impact factor: 11.025

3.  Autosomal dominant retinitis pigmentosa with apparent incomplete penetrance: a clinical, electrophysiological, psychophysical, and molecular genetic study.

Authors:  A T Moore; F Fitzke; M Jay; G B Arden; C F Inglehearn; T J Keen; S S Bhattacharya; A C Bird
Journal:  Br J Ophthalmol       Date:  1993-08       Impact factor: 4.638

4.  A gene for late-onset fundus flavimaculatus with macular dystrophy maps to chromosome 1p13.

Authors:  S Gerber; J M Rozet; D Bonneau; E Souied; A Camuzat; J L Dufier; P Amalric; J Weissenbach; A Munnich; J Kaplan
Journal:  Am J Hum Genet       Date:  1995-02       Impact factor: 11.025

5.  Evidence for a major gene (RP10) for autosomal dominant retinitis pigmentosa on chromosome 7q: linkage mapping in a second, unrelated family.

Authors:  R E McGuire; A M Gannon; L S Sullivan; J A Rodriguez; S P Daiger
Journal:  Hum Genet       Date:  1995-01       Impact factor: 4.132

  5 in total

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